Canonical Allele Identifier: CA200491647

Gene:

Linked Data

• dbSNP Id: rs59395779
• gnomAD v2: 9-132339068-G-A
• gnomAD v3: 9-129576789-G-A
• gnomAD v4: 9-129576789-G-A
• MyVariant Identifiers: chr9:g.132339068G>A (hg19) ; chr9:g.129576789G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.129576789G>A , CM000671.2:g.129576789G>A	GRCh38
NC_000009.11:g.132339068G>A , CM000671.1:g.132339068G>A	GRCh37
NC_000009.10:g.131378889G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_930390.1:n.182+1191G>A